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Establishing an experimental model of photodynamically induced anterior ischemic optic neuropathy
Numerous methods and drugs have been used to treat anterior ischemic optic neuropathy (AION); however, further investigations to determine the value of treatments for AION have been impeded by the lack of appropriate animal models of AION, significantly impacting on in-depth study of the disease. A...
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Published in: | Visual neuroscience 2011-03, Vol.28 (2), p.155-162 |
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description | Numerous methods and drugs have been used to treat anterior ischemic optic neuropathy (AION); however, further investigations to determine the value of treatments for AION have been impeded by the lack of appropriate animal models of AION, significantly impacting on in-depth study of the disease. A rat model of AION was established, and corresponding functional changes of the fundus were observed using fundus fluorescein angiography (FFA), optical coherence tomography (OCT), and flash visual-evoked potential (F-VEP) in order to confirm the reliability of the AION model histopathologically. One day after model establishment, histopathology demonstrated that portions of the optic disc were highly edematous, with edema of nerve fibers and loose tissue, accompanied by displacement of the surrounding retina. At 23 days, the optic disc and surrounding nerve fiber layers had become thinner. None of the above-mentioned changes was observed in the laser, hematoporphyrin derivative (HPD), or naive groups. The results of fundus, FFA, F-VEP, and OCT—within 90 days after model establishment—confirmed that krypton red laser irradiation (647 nm), applied 2 h after HPD injection, can establish an ideal animal model of AION. |
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A rat model of AION was established, and corresponding functional changes of the fundus were observed using fundus fluorescein angiography (FFA), optical coherence tomography (OCT), and flash visual-evoked potential (F-VEP) in order to confirm the reliability of the AION model histopathologically. One day after model establishment, histopathology demonstrated that portions of the optic disc were highly edematous, with edema of nerve fibers and loose tissue, accompanied by displacement of the surrounding retina. At 23 days, the optic disc and surrounding nerve fiber layers had become thinner. None of the above-mentioned changes was observed in the laser, hematoporphyrin derivative (HPD), or naive groups. The results of fundus, FFA, F-VEP, and OCT—within 90 days after model establishment—confirmed that krypton red laser irradiation (647 nm), applied 2 h after HPD injection, can establish an ideal animal model of AION.</description><identifier>ISSN: 0952-5238</identifier><identifier>EISSN: 1469-8714</identifier><identifier>DOI: 10.1017/S0952523810000398</identifier><identifier>PMID: 21356144</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><subject>Animals ; Biological and medical sciences ; Disease Models, Animal ; Evoked Potentials, Visual - physiology ; Eye and associated structures. Visual pathways and centers. Vision ; Fluorescein Angiography - methods ; Fundamental and applied biological sciences. Psychology ; Fundus Oculi ; Hematoporphyrins - adverse effects ; Lasers - adverse effects ; Male ; Optic Neuropathy, Ischemic - pathology ; Optic Neuropathy, Ischemic - physiopathology ; Papilledema - etiology ; Photosensitizing Agents - adverse effects ; Rats ; Rats, Sprague-Dawley ; Time Factors ; Tomography, Optical Coherence - methods ; Vertebrates: nervous system and sense organs ; Visual Fields - physiology</subject><ispartof>Visual neuroscience, 2011-03, Vol.28 (2), p.155-162</ispartof><rights>Copyright © Cambridge University Press 2011</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © Cambridge University Press, 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-e7f584dba552d821defd1f404fe140cf89bca087bed2b47c347b829909e0aa583</citedby><cites>FETCH-LOGICAL-c499t-e7f584dba552d821defd1f404fe140cf89bca087bed2b47c347b829909e0aa583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0952523810000398/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>315,786,790,27957,27958,73317</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24105040$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21356144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WANG, R.S.</creatorcontrib><creatorcontrib>LV, P.L.</creatorcontrib><creatorcontrib>WANG, W.J.</creatorcontrib><creatorcontrib>WANG, X.D.</creatorcontrib><creatorcontrib>ZHANG, X.J.</creatorcontrib><creatorcontrib>LI, S.N.</creatorcontrib><creatorcontrib>WANG, J.Z.</creatorcontrib><creatorcontrib>ZENG, Y.J.</creatorcontrib><title>Establishing an experimental model of photodynamically induced anterior ischemic optic neuropathy</title><title>Visual neuroscience</title><addtitle>Vis Neurosci</addtitle><description>Numerous methods and drugs have been used to treat anterior ischemic optic neuropathy (AION); however, further investigations to determine the value of treatments for AION have been impeded by the lack of appropriate animal models of AION, significantly impacting on in-depth study of the disease. A rat model of AION was established, and corresponding functional changes of the fundus were observed using fundus fluorescein angiography (FFA), optical coherence tomography (OCT), and flash visual-evoked potential (F-VEP) in order to confirm the reliability of the AION model histopathologically. One day after model establishment, histopathology demonstrated that portions of the optic disc were highly edematous, with edema of nerve fibers and loose tissue, accompanied by displacement of the surrounding retina. At 23 days, the optic disc and surrounding nerve fiber layers had become thinner. None of the above-mentioned changes was observed in the laser, hematoporphyrin derivative (HPD), or naive groups. The results of fundus, FFA, F-VEP, and OCT—within 90 days after model establishment—confirmed that krypton red laser irradiation (647 nm), applied 2 h after HPD injection, can establish an ideal animal model of AION.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Disease Models, Animal</subject><subject>Evoked Potentials, Visual - physiology</subject><subject>Eye and associated structures. Visual pathways and centers. Vision</subject><subject>Fluorescein Angiography - methods</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundus Oculi</subject><subject>Hematoporphyrins - adverse effects</subject><subject>Lasers - adverse effects</subject><subject>Male</subject><subject>Optic Neuropathy, Ischemic - pathology</subject><subject>Optic Neuropathy, Ischemic - physiopathology</subject><subject>Papilledema - etiology</subject><subject>Photosensitizing Agents - adverse effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Time Factors</subject><subject>Tomography, Optical Coherence - methods</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Visual Fields - physiology</subject><issn>0952-5238</issn><issn>1469-8714</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkU2L1TAUhoMozvXqD3AjRRBX1ZwmaZOlDOMHDLhQ1-U0OZnboU1q0oL335vLXB1QxCxOFud5z9fL2HPgb4BD9_YLN6pRjdDAyxNGP2A7kK2pdQfyIdud0vUpf8Ge5HzLOQhQ4jG7aECoFqTcMbzKKw7TmA9juKkwVPRjoTTOFFacqjk6mqroq-UQ1-iOAefR4jQdqzG4zZIrirXgMVVjtgcq2Soua4mBthQXXA_Hp-yRxynTs_O_Z9_eX329_Fhff_7w6fLddW2lMWtNnVdaugGVapxuwJF34CWXnkBy67UZLHLdDeSaQXZWyG7QjTHcEEdUWuzZ67u6S4rfN8prP5eZaJowUNxyr42BtpVg_k-2p1tKLgr58g_yNm4plDUKBMBFiQWCO8immHMi3y_lgJiOPfD-5FP_l09F8-JceBtmcr8Vv4wpwKszgLlc3CcMdsz3nASueBlxz8S5Oc5DGt0N3Y_47_Y_AS9Zqo0</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>WANG, R.S.</creator><creator>LV, P.L.</creator><creator>WANG, W.J.</creator><creator>WANG, X.D.</creator><creator>ZHANG, X.J.</creator><creator>LI, S.N.</creator><creator>WANG, J.Z.</creator><creator>ZENG, Y.J.</creator><general>Cambridge University Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20110301</creationdate><title>Establishing an experimental model of photodynamically induced anterior ischemic optic neuropathy</title><author>WANG, R.S. ; LV, P.L. ; WANG, W.J. ; WANG, X.D. ; ZHANG, X.J. ; LI, S.N. ; WANG, J.Z. ; ZENG, Y.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-e7f584dba552d821defd1f404fe140cf89bca087bed2b47c347b829909e0aa583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Disease Models, Animal</topic><topic>Evoked Potentials, Visual - physiology</topic><topic>Eye and associated structures. Visual pathways and centers. Vision</topic><topic>Fluorescein Angiography - methods</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundus Oculi</topic><topic>Hematoporphyrins - adverse effects</topic><topic>Lasers - adverse effects</topic><topic>Male</topic><topic>Optic Neuropathy, Ischemic - pathology</topic><topic>Optic Neuropathy, Ischemic - physiopathology</topic><topic>Papilledema - etiology</topic><topic>Photosensitizing Agents - adverse effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Time Factors</topic><topic>Tomography, Optical Coherence - methods</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Visual Fields - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WANG, R.S.</creatorcontrib><creatorcontrib>LV, P.L.</creatorcontrib><creatorcontrib>WANG, W.J.</creatorcontrib><creatorcontrib>WANG, X.D.</creatorcontrib><creatorcontrib>ZHANG, X.J.</creatorcontrib><creatorcontrib>LI, S.N.</creatorcontrib><creatorcontrib>WANG, J.Z.</creatorcontrib><creatorcontrib>ZENG, Y.J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Visual neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WANG, R.S.</au><au>LV, P.L.</au><au>WANG, W.J.</au><au>WANG, X.D.</au><au>ZHANG, X.J.</au><au>LI, S.N.</au><au>WANG, J.Z.</au><au>ZENG, Y.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Establishing an experimental model of photodynamically induced anterior ischemic optic neuropathy</atitle><jtitle>Visual neuroscience</jtitle><addtitle>Vis Neurosci</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>28</volume><issue>2</issue><spage>155</spage><epage>162</epage><pages>155-162</pages><issn>0952-5238</issn><eissn>1469-8714</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><notes>ObjectType-Article-2</notes><notes>ObjectType-Feature-1</notes><abstract>Numerous methods and drugs have been used to treat anterior ischemic optic neuropathy (AION); however, further investigations to determine the value of treatments for AION have been impeded by the lack of appropriate animal models of AION, significantly impacting on in-depth study of the disease. A rat model of AION was established, and corresponding functional changes of the fundus were observed using fundus fluorescein angiography (FFA), optical coherence tomography (OCT), and flash visual-evoked potential (F-VEP) in order to confirm the reliability of the AION model histopathologically. One day after model establishment, histopathology demonstrated that portions of the optic disc were highly edematous, with edema of nerve fibers and loose tissue, accompanied by displacement of the surrounding retina. At 23 days, the optic disc and surrounding nerve fiber layers had become thinner. None of the above-mentioned changes was observed in the laser, hematoporphyrin derivative (HPD), or naive groups. The results of fundus, FFA, F-VEP, and OCT—within 90 days after model establishment—confirmed that krypton red laser irradiation (647 nm), applied 2 h after HPD injection, can establish an ideal animal model of AION.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><pmid>21356144</pmid><doi>10.1017/S0952523810000398</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Disease Models, Animal Evoked Potentials, Visual - physiology Eye and associated structures. Visual pathways and centers. Vision Fluorescein Angiography - methods Fundamental and applied biological sciences. Psychology Fundus Oculi Hematoporphyrins - adverse effects Lasers - adverse effects Male Optic Neuropathy, Ischemic - pathology Optic Neuropathy, Ischemic - physiopathology Papilledema - etiology Photosensitizing Agents - adverse effects Rats Rats, Sprague-Dawley Time Factors Tomography, Optical Coherence - methods Vertebrates: nervous system and sense organs Visual Fields - physiology |
title | Establishing an experimental model of photodynamically induced anterior ischemic optic neuropathy |
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